In Vivo Pharmacokinetics/Pharmacodynamics of Cefquinome in an Experimental Mouse Model of Staphylococcus Aureus Mastitis following Intramammary Infusion.

Staphylococcus aureus remains the major cause of morbidity of bovine mastitis worldwide leading to massive economic losses. Cefquinome is a fourth generation cephalosporin, which preserves susceptibility and antibacterial activity against S. aureus. This work aims to study the pharmacokinetic (PK) and pharmacodynamic (PD) modeling following intramammary administration of cefquinome against S. aureus mastitis. The mouse model of S. aureus mastitis was developed for the PK/PD experiments. The plasma PK characteristics after intramammary injection of cefquinome at various single doses of 25, 50, 100, 200, 400 μg per gland (both fourth pairs of glands: L4 and R4) were calculated using one-compartment and first-order absorption model. PD study was investigated based on twenty-one intermittent dosing regimens, of which total daily dose ranged from 25 to 4800 μg per mouse and dosage intervals included 8, 12 or 24 h. The sigmoid Emax model of inhibitory effect was employed for PK/PD modeling. The results of PK/PD integration of cefquinome against S. aureus suggested that the percentage of duration that drug concentration exceeded the minimal inhibitory concentration (%T>MIC) and the ratio of area under time-concentration curve over MIC (AUC/MIC) are important indexes to evaluate the antibacterial activity. The PK/PD parameters of %T>MIC and AUC0-24/MIC were 35.98% and 137.43 h to obtain a 1.8 logCFU/gland reduction of bacterial colony counts in vivo, against S. aureus strains with cefquinome MIC of 0.5μg/ml.

Introduction

Bovine mastitis is an inflammation of the mammary glands usually resulted from bacterial colonization, consequence of yeast and even fungal or algae infection [1]. It can produce significant economic losses to the dairy industry due to quality deterioration of milk, dedication and veterinary care expenses and prohibitive labor costs for producers [1]. According to the clinical features, intramammary infection (IMI) is classified into two types: clinical mastitis and subclinical mastitis. Clinical mastitis is acute and severe, and may end up with death of patients. Subclinical mastitis (also called chronic mastitis) is rarely lethal but capable of resulting in a vast amount of financial losses. Staphylococcus aureus is the primary pathogen responsible for both forms of mastitis. Treatment of S. aureus mastitis is greatly difficult because the pathogen can release exotoxin, be resistant to many antimicrobials frequently, and survive in the intracellular space where the drug concentration is often low [1].

Cefquinome is a fourth generation cephalosporin applied as veterinary medicine solely. Cefquinome is stable to common plasmid- and chromosomally mediated beta-lactamases exhibiting antibacterial activity against a broad spectrum of Gram-positive and Gram-negative bacterial species. Most S. aureus isolates from bovine mastitis are susceptible to cefquinome [2-4]. The pharmacokinetic (PK) characteristics of cefquinome have been studied in various animals, such as, sheep, goats, cattle, buffalo calves, and camels via intravenous (i.v.) or intramuscular (i.m.) administration [5-9]. The PK profiles of cefquinome after local intramammary administration have also been performed in lactating cows and buffalo [10-12]. Previous report suggests that intramammary recipe is more successful than the systemic therapy, especially for Staphylococcal mastitis with a considerable microbiological cure rate [13,14]. The integration of PK/PD model has been widely applied in evaluation of antibacterial activity and optimization of dosing regimens. Although the PK fate of cefquinome and its efficacy of clinical treatment have been widely studied, there is no complete research linking the PK parameters to the PD effectiveness on mastitis therapy following various intramammary administration dosing regimens.

In the present study, we adopted the mouse model of S. aureus mastitis (MMSAM), which is popular in investigating the IMI and the treatment as an alternative model rather than practicing in target animal of cows [15]. This is because the costs related to the experimental IMI in cows are prohibitively high even to achieve the minimal power of statistical analysis [16]. Besides, the team has well studied this model through different aspects like pathology and application [16]. It is undeniable that possible differences between IMIs in two species, however results from this model may bring to light important mechanisms that could also take place during bovine mastitis caused by S. aureus. The objective of our experiment was to integrate PK/PD features and estimate the prime values of PK/PD parameters required for different levels of antibacterial efficacy.

Materials and Methods

Antimicrobial agents

Sterile powder of cefquinome for injection was purchased from Qilu Animal Health Products CO., LTD, Shandong, China. Stock solution of cefquinome was prepared in sterile water at 40,000 μg/ml and stored at -20°C till use. Working solutions were prepared daily by appropriate dilution of the stock solution with stroke-physiological saline solution (SPSS) and ultrapure water, respectively.

Bacterial strains and animals

S. aureus Newbould 305 (ATCC 29740), a mastitis isolates, was employed as the standard strain for experimental IMI of cows [17]. Thirty-eight S. aureus isolated from clinical bovine mastitis individuals in Inner Mongolia, China were also evaluated in this study. Broth and agar of Brain-Heart-Infusion (BHI), Mueller-Hinton (MH) and Mannitol Salt (MS) were purchased from Guangdong Huankai Microbial Sci. & Tech. CO., Ltd, Guangzhou, China.

All the lactating mice purchased from Vital River Laboratories, Beijing, China, with body weight ranged from 35 to 45 g, were bred in special-pathogen-free (SPF) environment, each two in one cage, with a 12: 12 light: dark circle and fed of SPF food (purchased from Southern Medical University, Guangzhou, China). All animal studies were approved by the Animal Use and Care Committee of South China Agricultural University and the guidelines of American Association for Accreditation of Laboratory Animal Care (AAALAC) were respected or followed during all the in vivo procedures [18].

MIC test

Susceptibility tests were determined according to Clinical and Laboratory Standards Institute (CLSI) guideline [19]. The MIC50 and MIC90 values were calculated, which represented the MIC value inhibiting the growth of at least corresponding 50% and 90% of isolates in a test population [20]. Triplet MIC tests were performed for all the strains and mean value of MIC was used for data analysis.

In vitro time-killing curves

An overnight culture of S. aureus Newbould 305 [17] was 10-fold diluted appropriately. Pathogens were exposed to five different cefquinome concentrations of 0.5×, 1×, 2×, 4× and 8× MIC and bred at 37°C with 200 rpm per minute shaking. Antibacterial activity against 2 initial inoculum of 106 and 107 CFU/mL were evaluated, respectively. Samples examined at 0, 3, 6, 9, and 24 h were subjected to 10-fold serial dilution and then plated onto MH agar for visible counts calculation. The detection limit was 100 CFU/ml. All the MH agar plates were cultured at 37°C for 22 to 24 h before colony counting.

Pharmacokinetics

The PK trials were performed in healthy CD-1 mice lactating for 10–12 days (six mice for each group). As we know, mouse has five pairs of mammary glands, three pairs on the thorax and two on the abdomen, which are identified by a letter and a number indicating their relative anatomic location from head to tail. Mastitis model are usually performed on L4 (fourth on the left) and R4 (fourth on the right) abdominal glands, because of their biggest size and easily to be harvested. Intramammary administration of a single dose cefquinome of 25, 50, 100, 200 or 400 μg/gland was injected into the L4 and R4 glands’ canals of mouse through a tiny cut at the end of teat using a 32-gauge blunt needle. Blood samples (about 50 μl at each time) were harvested by retro-orbital puncture at the following time points: 5 min, 10 min, 15min, 0.5 h, 0.75 h, 1 h, 2 h, 3 h, 4 h, 6 h, 8 h, and 12 h after administration. Plasma samples were obtained after centrifuging at 4000 rpm for 10 min. The drug concentrations in plasma were determined using the high-performance liquid chromatography—Electro-Spray Ionization—Mass Spectrometry (HPLC-ESI-MS/MS) method reported previously [21]. The linearity of cefquinome quantitation was within a range of 0.01–2 μg/ml and correlation coefficients were above 0.9999. The extraction recoveries of cefquinome from plasma was >90%, and coefficients of variation were <10% for both withinruns and between runs. The limit of quantification (LOQ) and detection (LOD) were 0.01 and 0.005 μg/ml, respectively. The PK parameters were calculated by the Winnonlin software (version 5.2.1, Pharsight, St. Louis, MO, USA), including half-lives of first-order absorption (T1/2ka) and elimination (T1/2Kel), area under time-concentration curve (AUC), the peak plasma concentration (Cmax), and the time of maximum concentration (Tmax).

The gland tissue samples were collected and mammary gland concentrations were tested, which data will be published separately.

The mouse model of S. aureus mastitis

The experimental conditions for mastitis model adopted here were similar to these as previously reported with minor modifications [16]. Briefly, 1 h following removal of 10–12 day-old offspring, lactating CD-1 mice (Vital River Laboratories, Beijing, China) were anaesthetized by intraperitoneal injection of 0.1 ml pentobarbital sodium (1.5%). A small cut at the end of teats was made to expose the mammary ducts and a 100 μl bacterial suspension containing about 4 × 103 CFU of S. aureus Newbould 305 (it should be noticeable that this final selection of bacterial inoculation is tailored to our pathogen isolates and animals used according to bacteriological, clinical and pathological evaluations) was injected through the teat canal using a 32-gauge aseptic blunt needle. The bacterial suspension was prepared from a serial dilution of an overnight culture in BHI broth. Control animals were inoculated with SPSS at the same volume. After inoculating, a 9 h incubation is required to allow the growth of bacterium to log phase. Then the mice were sacrificed and the L4 and R4 glands were aseptically harvested and homogenized in 3 ml SPSS to calculate the bacterium counts. The tissue suspension were evaluated for bacterial counts on MSA plates after serial 10-fold dilutions. The detection limit was 300 CFU/gland. The criterion of full preparation of MMSAM was the amount of bacteria reaching 106−7 CFU/gland, which is largely based on clinical and pathological evolutions. The number of animal ranged from 2 to 4 according to the different experiments.

In vivo growth and time-killing curves

Totally 180 mice were divided into five groups, growth control and four treatment groups of various regimens. Following the preparation of MMSAM, a single dose of 50, 100, 200, 400 μg/gland (i.e. 100, 200, 400, 800 μg per mouse) was intramammary administrated, respectively (recording as 0 h). Control group was treated with sterile SPSS. For this module, four mice were sacrificed and tested for bacterial CFU counts (i.e. 8 mammary glands) at each time point of 0, 1, 3, 6, 9, 12, 24 h, 48 h and 72 h.

PD experiments

S. aureus Newbould 305 was employed to determine the PD characteristics. After establishment of MMSAM, tested mice were divided into twenty-one groups treated with cefquinome under various dosing regimens. The dosage two-fold increased from 12.5 to 800 μg/gland and the dosing intervals were 8, 12 and 24 h (once, twice and thrice a day), respectively. Control group was treated with sterile SPSS. After the 24 h treatment, 4 mice a group (i.e. n = 8 for gland) of each dosing regimen were euthanized. The L4 and R4 glands were then harvested for bacterial CFU counts. The control group was sacrificed before the intramammary administration and at 24 h.

PK/PD analysis

The PK/PD parameters of the 21 regimens were extrapolated from the corresponding single dosing PK data obtained above. The surrogate markers of antibacterial efficacy included the ratio of area under the concentration time curve to the MIC for 0 to 24 h (AUC0-24/MIC), the duration of drug concentration exceeding the MIC (%T > MIC) and the peak concentration divided by the MIC (Cmax/MIC). MIC90 value was employed for formulation of PK/PD indexes. The %T>MIC, AUC0-24, and Cmax for multiple dosing regimens are calculated using following eq 1: Where C is the concentration drug concentration, n is the dosing times, Ka is the absorption half-life, F is the bioavailability, V is the apparent volume of distribution, X0 is the dose of antibiotic, Kel is the elimination half-life and τ is the dosing interval. The PK parameter of Ka, Kel, and F/V are achieved in PK test mentioned above.

PK/PD integration

The antimicrobial effect of cefquinome was analyzed by applying the sigmoid Emax model of inhibitory effect, as previously reported [22], which is defined as eq 2: where E is the antibacterial effect, measured as the change in the bacterial counts (logCFU/gland) in the gland sample after 24 h of treatment compared to the initial colony counts; E is the ΔlogCFU24h in the drug-free control sample; E is the ΔlogCFU24h in the test sample containing cefquinome, when the maximum antibacterial effect was achieved; C is the PK/PD index (AUC0-24/MIC, Cmax/MIC or %T > MIC for serum drug concentration); EC is the value of PK/PD index of drug producing 50% of the maximum antibacterial effect; and N is the Hill coefficient, which describes the steepness of the effect curve resulting from each PK/PD indices.

Results

MICs of cefquinome against S. aureus Newbould 305 and mastitis isolates

Cefquinome MICs were 0.5 μg/ml against S. aureus Newbould 305 and 0.25 to 0.5 μg/ml against the thirty-eight isolates, with MIC50 and MIC90 both of 0.5 μg/ml (S1 Table).

In vitro time killing curves of cefquinome against different inoculum load

The in vitro time-killing curves against S. aureus Newbould 305 is presented in Fig 1. The killing profile of cefquinome showed low correlation with the exposed dose, as the killing speed did not change with the increasing drug concentration. At 2× MIC and all higher concentrations, bactericidal activity of 3.5 and a less than 3 logCFU/ml kill were observed against 106 initial inoculum group and 107 initial inoculum group, respectively. Cefquinome concentration less than MIC cannot inhibit the bacterial growth.

Fig 1

In vitro time-killing curves of cefquinome against S. aureus Newbould 305 with cefquinome MIC of 0.5 μg/ml.

The cefquinome concentrations of 2×, 4×, and 8×MIC exhibited a same killing speed and actability, by reducing 2.5–3 logCFU/ml of bacterial colony during 9 h incubation. A and B shows different antibacterial activity against different initial bacterial load (106 log10CFU/mL and 107 log10CFU/mL). Each symbol represents mean value and bars represent standard deviations.

Plasma PK of cefquinome

No adverse effects (including death of stress, acute death, depression, and abnormal behavior) were observed after intramammary administration. The plasma drug concentration data are considered largely for free drug since the low protein binding rate (17% in the mouse) [23] and the way we handle the sample preparation protein precipitation. The semi-logarithmic plots of plasma concentration-time curves for various dosages are shown in Fig 2. The one-compartment model with first-order absorption was the best-fit model to calculate the relevant PK parameters, as the Akaike Information Criterion (AIC) was the lowest. The Tmax ranged from 0.17 to 0.27 h with a mean value of 0.22 h. T1/2Kel of plasma varied from 0.34 to 0.49 h with an average of 0.4 h. Cmax and AUC increased with dosage linearly (Table 1).

Fig 2

Semi-logarithmic plot of serum concentration versus time of cefquinome mouse model of S. aureus mastitis (n = 6), following a single intramammary administration dose of 25, 50, 100, 200, or 400 μg/gland.

Bars represent standard deviations. Horizontal dotted line represents the MIC90 value of 38 isolates.

Table 1

PK parameters of cefquinome in plasma after intramammary administration analyzed by one-compartment model with first-order absorption (n = 6).

Variable(units)	Intramammary administration dose (μg/gland)
	25	50	100	200	400	Mean ± SD
T1/2Ka (h)	0.07±0.01	0.07±0.02	0.11±0.04	0.08±0.02	0.05±0.01	0.08 ± 0.02
T1/2Kel (h)	0.49±0.08	0.41±0.1	0.34±0.12	0.35±0.06	0.39±0.07	0.4 ± 0.06
Tmax (h)	0.22±0.02	0.21±0.03	0.27±0.03	0.22±0.02	0.17±0.02	0.22 ± 0.03
AUC (μg·h/ml)	0.99±0.08	2.55±0.31	4.93±0.55	8.03±0.52	18.57.28±1.9	NA
Cmax (μg/ml)	1.03±0.04	3.02±0.17	5.83±0.32	10.29±0.33	24.33±1.02	NA

T1/2Ka, absorption half-life; T1/2Kel, elimination half-life; AUC, area under plasma concentration-time curve of 0 to 4 h; Tmax, time of maximum concentration; Cmax, maximum concentration; (n = 6).

Establishment of MMSAM and in vivo time-killing curves

Acute clinical mastitis of bacterial colony counts reaching 107 CFU was achieved by intramammary injection of 100 μl suspension containing about 4000 CFU and incubation for 9 h. The steady phase of colonization about 109 CFU was found during 24 h and 48 h incubation (S1 Fig).

The in vivo time-killing course are shown in Fig 3. In the control group, initial colony counts was 7.76 logCFU/gland and increased to 10.29 logCFU/gland at 24 h. The killing speed of cefquinome in MMSAM was slower than that in broth medium in vitro. At dose of 200 and 400 μg/gland, an antibacterial activity, about 2.3 logCFU/gland reduction was observed after 24 h incubation, while no net change of bacteria load at dose of 50 and 100 μg/gland cefquinome was observed at 24 h. After a single dose, bacterial regrowth was observed in the four groups at 72 h.

Fig 3

Changes in viable cell density (CFU/gland) of S. aureus and concentrations of antibiotics (×MIC) in vivo following a single treatment with cefquinome.

Testing dosing regimens were single doses at 50, 100, 200 and 400 μg/gland by intramammary administration, (n = 4 for mice, i.e. for glands n = 8).

PD effectiveness of 21 dosing regimens

The treatment activity of cefquinome was evaluated by the net change of bacterial counts (logCFU/gland) during 24 h in MMSAM. Before administration, strains’ population reached 7.61 logCFU/gland (mean value) in the inoculated mammary. The bacterial load at 24 h after treatment were shown in S2 Fig. When given a dose above 400 μg/gland and with 8 or 12 h dosing intervals, a better antibacterial activity was observed with more than 2 logCFU/gland reduction versus 1 log for 200 μg/gland (P<0.05, two-tailed t-test). As the dose level and the dosing interval increased, the in vivo antibacterial activity of cefquinome was elevated, exhibiting a declining trend of survival strains’ population by the end of the experimental circle.

PK/PD Integration

The PK/PD parameters of multiple dosing regimens are reported in S2 Table, regarding the regimens in PD experiments for which no kinetics were determined.

The PK/PD profiles of plasma concentrations versus antibacterial effect were analyzed by the sigmoid E model of inhibitory effect (Fig 4). The correlation coefficient (R) between antibacterial effects and %T>MIC and AUC0-24/MIC were 0.8466 and 0.908, accordingly. The PD parameters of E, E, PK/PD parameters required for various degrees of antibacterial activity and the Hill coefficient N are presented in Table 2.

Fig 4

Sigmoid Emax relationships between in vivo antibacterial effect (△logCFU24h/gland) and PK/PD indexes of %T>MIC and AUC0-24/MIC against S. aureus Newbould 305.

The lines represent the model fits of the data. R is the correlation coefficient.

Table 2

Integration of PK/PD after intramammary administration of cefquinome in mouse model of S. aureus mastitis.

Parameter	Value (Mean ± SD)
	%T>MIC	AUC/MIC
Log Emax (logCFU/gland)	2.94±0.19	3.00±0.15
Log E0 (logCFU/gland)	-2.11±0.22	-2.04±0.13
Log Emax—Log E0 (logCFU/gland)	5.05±0.33	5.03±0.22
EC50 (h)	6.12±0.49	4.44±0.45
For bacteriostatic action (h)	7.59±0.03	6.91±0.10
For 1.8 logCFU reduction (h)	35.98±0.03	137.43±0.10
Slope (N)	1.54±0.19	0.88±0.07

Emax, the difference in the bacterial number in the control sample (drug-free) after 24 h incubation from initial inoculum (△logCFU24h/gland); E0, △logCFU24h/gland in the test sample containing cefquinome after 24 h incubation when the best antibacterial activity is reached; EC, the value of PK/PD parameters when the half effect is achieved; N, the Hill coefficient.

PK/PD Model Parameter Estimates for the Target Efficacy

The target values of cefquinome necessary to produce a bacteriostatic action and a 1.8-log10-CFU/gland reduction were 7.59% and 35.98% for %T>MIC and 6.91 and 137.43 h for AUC0-24/MIC, respectively.

Discussion

In present study, the MICs of cefquinome against S. aureus Newbould 305 and clinical bovine mastitis isolates ranged from 0.25 to 0.5 μg/ml, which are in line with the values previously reported [23]. As a fourth-generation of cephalosporin, cefquinome maintain a remarkable antibacterial potential, since different species or strains causing mammary inflammation and gland tissue damages express the susceptibility to this drug in general [2-4]. Besides, we demonstrated that cefquinome was fairly effective, causing an over 3-log10-unit reduction of bacterial load in time-killing curves in vitro, suggesting a bactericidal activity of cefquinome.

In addition, several issues need to be illustrated. Firstly, according to PK study the absorption half-life (t1/2ka) of 0.09 ± 0.03 h was slightly shorter than 0.14 h for i.m. and 0.29 h for s.c. in beagle dogs [21]. After intramammary administration, a rapid absorption phase was observed like other administrating routes (subcutaneous or intramuscular) and tmax of 0.24 ± 0.04 h in this work is in agreement with 0.3 h in mice [23] and 0.25 h in rabbits in previous report [24]. The elimination half-life was 0.44 ± 0.09 h, similar to previous study of 0.37 h, revealing a fast eliminating from blood circulation system [23]. A similar PK profiles of healthy quarter, infected quarter and suspected quarter were reported in previous literature, by which a negligible influence of the udder environment was claimed [12].

Secondly, in this work, the inoculum amounts of S. aureus strains were large enough to imitate the acute and severe intramammary infection, which was approximate of 7.5~8 logCFU/gland right before the drug administration. The initial massive bacterial load increased the burden of antibacterial activity of cefquinome, as a result dosages of 100 μg/gland or lower can only inhibit the growth of bacterium (slightly change in CFU) rather than killing of any (reduction of bacteria counts) at 24 h. In the 400 and 200 μg/gland single dose groups, 2.88 and 2.4 logCFU/gland differences of bacterial counts were observed at 24 h, respectively. Nevertheless, the antibacterial effects were similar (P > 0.05, two-tailed t-test). In addition, a single dose of 200 or 400 μg/gland cannot inhibit the bacterial regrowth after 72 h following administration. Thus, we can tell that it is difficult to achieve a bactericidal activity of 99.9% reduction of total bacteria in vivo, as the condition in vivo was much more complex than in culture medium. In vivo, drug concentration was ever changing and distribution of cefquinome was mainly in the extracellular fluid. But survival in both extracellular and intracellular were observed for S. aureus strains [25]. On the other hand, Staphylococcal infections do not always readily respond to antibiotic treatment and the pathogen can survive in the host in an attenuated form called small-colony variants, against which many antibiotics are not effective even they can penetrate mammalian cells [26].

To explore as widely as possible the potential clinical range, concentration range and therapeutic range in clinical situation, 21 regimens comprised of 7 doses and 3 dose intervals are investigated. From previous researches, the killing characteristic of cefquinome is time-dependent [8,23], and there is no doubt that %T>MIC is an essential parameter to describe the antibacterial activity with R of 0.8466.

However, an interesting outcome drew our attention. The influence of AUC0-24/MIC on treatment effectiveness is distinguished and considerable as well as the %T>MIC. For example, in time course killing trials, the in vivo antibacterial pattern of cefquinome has changed and been different from that in vitro (Figs 1 and 3). As the bolus dose increasing, the bacterial counts in gland tissue has dropped after 24 h observation, which suggests a dose related killing activity in vivo. Although the R of 0.908 for AUC/MIC is greater than %T>MIC numerically, the statistical significance evaluation is not available. Similarly, a dose-dependent manner of bacterial counts reduction in gland was observed following intramuscular and intravenous injections of cephapirin in the treatment of mouse mastitis [15]. Otherwise, the parameter of AUC/MIC is utilized to represent the pattern of antibacterial activity of time-dependent killing and prolonged persistent effect [27], and it combines both time and drug concentration factors with bacterial killing efficacy. In addition, the diffusion of cefquinome between blood and mammary gland, known as the blood-milk barrier, is limited. Drug distribution between blood and gland may not be identical when being compared to that between blood and thigh or among blood and lung tissues. Due to these reasons, the %T > MIC and AUC0-24/MIC are considered both to be important for the antibacterial efficacy.

It is not uncommon that an antibiotic drug’s PK/PD parameter could be more than one. For example, levofloxacin therapy in pulmonary, soft tissue, and urinary infections, two PK/PD parameters of Cmax/MIC and AUC/MIC were found to be essential predictors for its therapeutic effect [28]. In the present work, the significance of AUC/MIC index has elevated and both %T > MIC and AUC0-24/MIC are important following intramammary administration. Although non-target animal studies are not able to directly define the optimal clinical dose regimen when considering the species difference, they are still capable of defining the magnitude of the PK/PD index required for different treatment outcomes since various animal species including human should share a similar magnitude of the PK/PD index [27,29].

Conclusions

To our knowledge, this is the first study applying a PK/PD model in IMI treatment. The activity of cefquinome against S. aureus was investigated through a mouse mastitis model. In conclusion, according to the integration of PK/PD, the parameters of %T>MIC and AUC0-24/MIC are important and may be mainly responsible for the prediction of antibacterial efficacy and the treatment outcomes of cefquinome after intramammary administration. Moreover, clinical dosing regimens may satisfy the %T>MIC and AUC0-24/MIC equals to or exceeds the value of 35.98% and 137.43 h so as to achieve a good antibacterial effect against S. aureus strains with an MIC of 0.5 μg/ml. Understanding the complexity of across species extrapolation of PK/PD data, the present study should be regarded as work providing rational understanding and some essential data for PK/PD evaluation aiming at optimizing bovine mastitis treatment strategy via intramammary drug administration.

In vivo growth curve in mouse model of S. aureus mastitis.

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The Bacterial colony count (log10 CFU/mL) in mammary gland following treatments of 21 dosing regimens.

The dose ranged from 12.5 to 800 μg/gland and dosing intervals were 8, 12, and 24 h.

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MICs of cefquinome against 38 clinical isolates.

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PK/PD parameters of 21 regimens following intramammary administration.

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